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Overview The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together seven national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system. The Business Entities under CRIS include: Singapore Clinical Research Institute (SCRI)Advanced Cell Therapy and Research Institute, Singapore (ACTRIS)Cardiovascular Disease National Collaborative Enterprise (CADENCE)Together, CRIS makes a positive difference to Singapore patients and researchers by ensuring that these clinical research platforms and programmes are at the cutting edge of capability development and innovation. If you are as passionate as we are in clinical trials and research, we want youCADENCE The Cardiovascular Disease National Collaborative Enterprise (CADENCE) is a national program for Cardiovascular Research that aims to strengthen the overall impact of cardiovascular research and translation in Singapore through: (1) synergising efforts across Singapore through the establishment of Joint Platforms to improve patient outcomes and establish Singapore as a global leader in cardiovascular disease (CVD) research; (2) overcoming common barriers to research at the systems level; (3) driving commercialisation efforts; and (4) demonstrating the power of these synergies through a series of practice-changing Use Cases. CADENCE will be housed as a business unit within the Consortium for Clinical Research and Innovation Singapore (CRIS), a wholly-owned subsidiary of the Ministry of Health Holdings (MOHH) Pte Ltd and anchored by the CVD research programmes and commercialization platforms of partner institutions (MOHT, NHCS & NHRIS, NUHCS & CVRI, NHG Heart Institute, KTPH, A*STAR, NUS, Duke-NUS, LKC). What you will be working on The Clinical Research Coordinator (CRC) will be seconded to the public healthcare institution to support research/trials under CADENCE flagship program by: Supporting the investigators in the conduct and implementation of clinical research/trial activities. Providing administrative support to activities related to clinical research/trial implementation. Major Duties or Responsibilities Support the investigators in coordinating clinical research activities from study start up, screening, recruitment till study closure which includes but not limited to: Managing research project as assigned independently. Act as liaison between subjects and study teams to facilitate and coordinate the study activities inaccordance to protocol requirements. Assist Project Investigators (PI) in designing and development of study related documents including study specific sourcedocuments, data collection forms, recruitment advertisement and other required documentspertaining to the protocol. Assist sponsor and/or PI in submissions to IRB and/or HSA. Oversees all study subject relatedissues and ensure timely reporting of all safety events in accordance to sponsor, IRB and regulatory requirements. Provide regular study updates to study teams and sponsors. Perform data collection and entry accurately in a timely manner. Assist in study budget drafting. Develop and maintain accurate and timely update of financial tracker. Prepare and ensure that subjects' reimbursement is performed timely. Verify study
